Evidence map›Paper›PMID 36558992›Full record

ArticlePharmaceuticals (Basel, Switzerland)2022

A Mechanism of Isoorientin-Induced Apoptosis and Migration Inhibition in Gastric Cancer AGS Cells.

Tong Zhang, Yun-Hong Xiu, Hui Xue, Yan-Nan Li, Jing-Long Cao, Wen-Shuang Hou, Jian Liu, Yu-He Cui, Ting Xu, Ying Wang and 1 more

Open access · goldAbstract read
In one paragraph

Article in Pharmaceuticals (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed, 1 pooled it
2.9field-weighted citation impact, top 9% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

12 citing papers in PubMed, 1 synthesis or guideline pooled it, 16 citations in OpenAlex.

  1. Natural flavonoid isoorientin and its anticancer mechanisms: a systematic review.Naunyn-Schmiedeberg's archives of pharmacology · 2026
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 2 institutions in 1 country.

Tong ZhangCollege of Life Science & Technology, Heilongjiang Bayi Agricultural University, Daqing 163319, China.
Yun-Hong XiuHemodialysis Center, Daqing Oilfield General Hospital, Daqing 163001, China.
Hui XueCollege of Life Science & Technology, Heilongjiang Bayi Agricultural University, Daqing 163319, China.
Yan-Nan LiCollege of Life Science & Technology, Heilongjiang Bayi Agricultural University, Daqing 163319, China.
Jing-Long CaoCollege of Life Science & Technology, Heilongjiang Bayi Agricultural University, Daqing 163319, China.
Wen-Shuang HouCollege of Life Science & Technology, Heilongjiang Bayi Agricultural University, Daqing 163319, China.
Jian LiuCollege of Life Science & Technology, Heilongjiang Bayi Agricultural University, Daqing 163319, China.
Yu-He CuiCollege of Life Science & Technology, Heilongjiang Bayi Agricultural University, Daqing 163319, China.
Ting XuCollege of Life Science & Technology, Heilongjiang Bayi Agricultural University, Daqing 163319, China.
Ying WangNational Coarse Cereals Engineering Research Center, Daqing 163319, China.
Cheng-Hao JinCollege of Life Science & Technology, Heilongjiang Bayi Agricultural University, Daqing 163319, China.
Heilongjiang Bayi Agricultural University · CNDaqing Oilfield General Hospital · CN

Funding

Central Government Supports Local College Reform and Development Fund Talent Training Projects 2020GSP16Heilongjiang Touyan Innovation Team Program 2019HTY078National Key Research and Development Project of China 2020YFD1001400
6 · The paper itself

Abstract

Isoorientin (ISO) is a flavonoid compound containing a luteolin structure, which can induce autophagy in some tumor cells. This study investigated the impact of ISO in gastric cancer AGS cells, and performed an experimental analysis on the main signaling pathways and transduction pathways it regulates. CCK-8 assay results showed that ISO reduced the survival rate of gastric cancer AGS cells, but the toxicity to normal cells was minimal. Hoechst 33342/PI double staining assay results showed that ISO induced apoptosis in gastric cancer AGS cells. Further analysis by flow cytometry and Western blot showed that ISO induced apoptosis via a mitochondria-dependent pathway. In addition, the level of reactive oxygen species (ROS) in gastric cancer AGS cells also increased with the extension of the ISO treatment time. However, cell apoptosis was inhibited by preconditioning cells with N-acetylcysteine (NAC). Moreover, ISO arrested the cell cycle at the G2/M phase by increasing intracellular ROS levels. Cell migration assay results showed that ISO inhibited cell migration by inhibiting the expression of p-AKT, p-GSK-3β, and β-catenin and was also related to the accumulation of ROS. These results suggest that ISO-induced cell apoptosis by ROS-mediated MAPK/STAT3/NF-κB signaling pathways inhibited cell migration by regulating the AKT/GSK-3β/β-catenin signaling pathway in gastric cancer AGS cells.

Indexed as

cell apoptosiscell cyclecell migrationgastric cancerisoorientinreactive oxygen species

Identifiers

PMID36558992
PMCPMC9788167
OpenAlexW4311397311

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.